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Bioorganic & Medicinal Chemistry Letters|June 17, 2008
(D)-2-tert-Butoxycarbonylamino-5,5-difluoro-5-phenyl-pentanoic acid: synthesis and incorporation into the growth hormone secretagoguesJun Li, Stephanie Y Chen, Brian J Murphy, et al.Bioorganic & Medicinal Chemistry Letters|March 23, 2005
Tetrahydroisoquinoline 1-carboxamides as growth hormone secretagoguesJames J Li, Haixia Wang, Fucheng Qu, et al.The Journal of Pharmacology and Experimental Therapeutics|March 3, 2009
Enhanced gastrointestinal motility with orally active ghrelin receptor agonistsSoratree Charoenthongtrakul, Derek Giuliana, Kenneth A Longo, et al.Bioorganic & Medicinal Chemistry Letters|April 2, 2008
Tetrazole based amides as growth hormone secretagoguesJames J Li, Haixia Wang, Jun Li, et al.Bioorganic & Medicinal Chemistry Letters|February 20, 2008
Optimization of 1H-tetrazole-1-alkanenitriles as potent orally bioavailable growth hormone secretagoguesAndrés S Hernández, Stephen G Swartz, Dorothy Slusarchyk, et al.Bioorganic & Medicinal Chemistry Letters|March 27, 2007
2-hydroxy-N-arylbenzenesulfonamides as ATP-citrate lyase inhibitorsJames J Li, Haixia Wang, Joseph A Tino, et al.Bioorganic & Medicinal Chemistry Letters|September 18, 2007
Discovery, synthesis, and structure-activity studies of tetrazole based growth hormone secretagoguesAndrés S Hernández, Peter T W Cheng, Christa M Musial, et al.Journal of Medicinal Chemistry|August 27, 2016
Synthesis and Antiobesity Properties of 6-(4-Chlorophenyl)-3-(4-((3,3-difluoro-1-hydroxycyclobutyl)methoxy)-3-methoxyphenyl)thieno[3,2-d]pyrimidin-4(3H)-one (BMS-814580): A Highly Efficacious Melanin Concentrating Hormone Receptor 1 (MCHR1) InhibitorSaleem Ahmad, William N Washburn, Andres S Hernandez, et al.Bioorganic & Medicinal Chemistry Letters|February 26, 2008
Design and synthesis of tetrazole-based growth hormone secretagogue: the SAR studies of the O-benzyl serine side chainJun Li, Stephanie Y Chen, Shiwei Tao, et al.Bioorganic & Medicinal Chemistry Letters|February 10, 2009
Design, synthesis and structure-activity relationships of azole acids as novel, potent dual PPAR alpha/gamma agonistsHao Zhang, Denis E Ryono, Pratik Devasthale, et al.Pageof 3